Home  Contacts  Order  Catalog  Support
 Search  Alphabetical Index  Numerical Index
 Restriction Enzymes  Modifying Enzymes  PCR, qPCR, RT-PCR & dNTPs  Molecular Cloning  Nucleic Acid Purification
 Molecular Labeling & Detection  In vitro Transcription  Electrophoresis Products  Nucleotides  Transfection Reagents  Reagents
C A T A L O G
 

Eam1105I (AhdI)
Available in FastDigest® format

5'-G A C N N N^N N G T C-3'
3'-C T G N N^N N N C A G-5' 

digested lambda DNA
0.7% agarose
      
#ER0241
Supplied with:
10X Buffer Eam1105I
10X Buffer Tango™
1000 u
 
1 ml
1 ml
#ER0242
Supplied with:
10X Buffer Eam1105I
10X Buffer Tango™
5000 u
 
2x1 ml
1 ml
Commercial Isoschizomers:
AhdI, AspEI, BmeRI, DriI, EclHKI

Related Documents (in pdf, ~55 KB):

Certificate of Analysis: #ER0241, #ER0242
MSDS (English)
MSDS (English-USA)
MSDS (German)
Chart (in pdf, 721 KB)
Brochure (in pdf, 316 KB)

Concentration
10 u/µl

Conditions for 100% Activity

Recommended
buffer
Incubation
temperature
Units for 
overnight 
incubation,
u/µg DNA
Thermal
inactivation,
in 20 min

Enzyme activity, %

Eam1105I
(unique)

(blue)

(green)

(orange)

(red)
Tango™ 
(yellow)
1X 1X 1X 1X 1X 1X 2X
Buffer Eam1105I 37°C 0.1 65°C 100 20-50 50-100 0-20 0-20 50-100 20-50

Storage Buffer
10 mM Tris-HCl (pH 7.4 at 25°C), 100 mM KCl, 1 mM DTT, 1 mM EDTA, 0.2 mg/ml BSA and 50% glycerol.

Ligation and Recutting
After 10-fold overdigestion with Eam1105I, more than 80% of the digested DNA fragments can be ligated in a reaction mixture containing 20-40 u of T4 DNA Ligase/1 µg of fragments and 10% PEG. More than 90% of these can be recut.

Methylation Effects
Dam:
Dcm:
CpG:
EcoKI:
EcoBI:
 never overlaps
 never overlaps
 may overlap
 never overlaps
 never overlaps
- no effect.
- no effect.
- no effect.
- no effect.
- no effect.

Digestion of Agarose-embedded DNA
Minimum 5 units of the enzyme are required for complete digestion of 1 µg of agarose-embedded lambda DNA in 16 hours.

Note
Low salt, high glycerol (>5%) concentrations, pH >8.0 or large excess of the enzyme may result in star activity.

Double Digestions using Tango™ Buffer, DoubleDigest™

Optimal
buffer

Enzyme activity, %

Tango™ 
(yellow)
1X 2X
Buffer Eam1105I 50-100 20-50

Number of Recognition Sites in DNA Molecules

Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184
9 1 0 1 1 1 1 1 1 1 1

See also General Properties of Restriction Enzymes:

 

 Home  Search  Contacts  Order  Catalog  Support

Updated balandžio 22, 2008 11:22